US4501858A - Accelerators for vulcanizing vinylidene fluoride elastomeric copolymers - Google Patents

Accelerators for vulcanizing vinylidene fluoride elastomeric copolymers Download PDF

Info

Publication number
US4501858A
US4501858A US06/591,994 US59199484A US4501858A US 4501858 A US4501858 A US 4501858A US 59199484 A US59199484 A US 59199484A US 4501858 A US4501858 A US 4501858A
Authority
US
United States
Prior art keywords
vinylidene fluoride
sup
vulcanization
vulcanizing
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US06/591,994
Other languages
English (en)
Inventor
Giovanni Moggi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Montedison SpA
Original Assignee
Montedison SpA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Montedison SpA filed Critical Montedison SpA
Assigned to MONTEDISON S.P.A. reassignment MONTEDISON S.P.A. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: MOGGI, GIOVANNI
Application granted granted Critical
Publication of US4501858A publication Critical patent/US4501858A/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/5399Phosphorus bound to nitrogen

Definitions

  • vulcanized elastomers based on vinylidene fluoride copolymers are well known and are widely employed in a plurality of applicative fields where an exceptional chemical resistance to solvents, lubricants, fuels, acids and the like, even at very high temperatures, is required.
  • vulcanizing agents of polynucleofilic compounds and in particular of aromatic polyhydroxyl compounds (or of similar thioderivatives), either as such or in the salified form.
  • Another object is that of providing a process for vulcanizing compositions based on vinylidene fluoride elastomeric copolymers, which is free from the shortcomings cited hereinabove and is capable of providing vulcanized articles exhibiting a high adhesion to metal substrates.
  • a third object is also that of providing vulcanized compositions based on vinylidene fluoride elastomeric copolymers, free from the drawbacks mentioned in the foregoing, and which may be shaped by injection molding.
  • compositions comprising:
  • fluorinated or chlorofluorinated ethylenically unsaturated monomers such as e.g. 1-hydropentafluoropropene; 2-hydropentafluoropropene; 1,1-dihydrotetrafluoropropene, partially or thoroughly fluorinated alkyl- and arylvinylethers, and the like;
  • an inorganic acid acceptor consisting of one or more basic oxides of divalent metals, selected from the group comprising magnesium oxide, calcium oxide, lead monoxide, zinc oxide and/or of one or more basic lead phosphites, optionally in the form of cationic complexes or chelates;
  • A is an arylene radical, n is an integer equal to or higher than 2, B is oxygen or sulphur; C is hydrogen or an alkaline metal, R is an alkylene or cycloalkylene, mono- or polyalkylenecycloalkyl, or alkylenediaryl or oxoalkylenediaryl radical;
  • the vulcanizable compositions of the type specified hereinabove are vulcanized by means of a process, which too is an object of the present invention, that consists in first heating said compositions, under pressure, to temperatures in the range from 130° C. to 230° C., preferably from 160° C. to 200° C., during a time from 0.5 to 60 and preferably from 1 to 20 minutes; the articles so obtained are successively postvulcanized in an oven or a furnace, at atmospheric pressure, at temperature ranging from 130° C. to 315° C., preferably from 200° C. to 275° C., for a period of time from 5 to 48 and preferably from 10 to 24 hours.
  • the vulcanizable compositions according to this invention can be transformed into articles of any shape and size by extrusion molding and subsequent vulcanization, employing also highly automatized injection technologies; in fact, at the high temperatures which are usual for the injection molding process, no drawbacks occur due to scorching or hot tearing phenomena.
  • Such articles exhibit an excellent resistance to permanent set and to compression, a minimum tendency to scorching as a function of the storing time and temperature or of the temperatures of particular processing technologies, such as for example the extrusion, and also a high resistance to thermal ageing; furthermore, they can be bonded to metal substrates of different types, to which they exhibit a considerable adhesion even at high temperatures.
  • the process according to the present invention is particularly suitable in the case of copolymers containing from 30 to 70% by moles of vinylidene fluoride and from 70 to 30% by moles of 1-hydropentafluoroprene and/or hexafluoropropene, or in the case of vinylidene fluoride/tetrafluoroethylene/hexafluoropropene and/or 1-hydropentafluoropropene terpolymers, in which the percent amounts of the three monomers respectively range from 40 to 80, from 30 to 10 and from 30 to 10% by moles.
  • the process according to the present invention is advantageously utilizable for all the fluorinated polymeric materials of the elastomeric type, optionally containing substituents other than fluorine and chlorine, and also for the mixtures of two or more fluorinated elastomers.
  • Preferred compounds to be used according to the present invention as vulcanization accelerators are:
  • this compound is prepared from equimolar amounts of A 1 and of sodium tetrafluoroborate in aqueous solution.
  • the product precipitates in the form of very fine white crystals having a melting point of 233° C.;
  • a 6 [(C 6 H 5 ) 3 P] 2 NB(C 6 H 5 ) 4
  • the accelerator amount to be employed in the process according to the present invention depends on whether or not steric hindrances are present in the additive, on the basicity degree of the vulcanizable composition and on many other factors connected with the other particular additives utilized, on the type, shape and dimensions of the article to be manufactured, on the vulcanization conditions and on the heating system and modalities during vulcanization.
  • the vulcanizable compositions according to the present invention may contain, in addition to the substances indicated hereinbefore from (I) through (V), carbon black, white and coloured fillers, plasticizers and lubricants already known, such as stearates, arylphosphates, polyethers, polyesters, polyethylene and other known additives, according to the techniques usually employed by the fluorinated elastomers users.
  • the components of the vulcanizable compositions of the present invention are easy to incorporate into the vinylidene fluoride elastomeric copolymer, both separately and premixed, or they may be solubilized in solvents and then caused to be adsorbed on inert fillers having a large surface area, without giving rise to any undesired accompanying phenomenon, such as surface efflorescence, caused by migration phenomena inside the vulcanizable composition, due to the high compatibility with the elastomer.
  • Another advantage according to the present invention consists in the complete elimination of the undesired "back rinding" phenomena during vulcanization in closed mold and under pressure of articles prepared from fluorinated elastomers, particularly in the case of O-ring gaskets.
  • the mixture of bis(triarylphosphin)-iminium salt (0.1-2 parts by weight) and of vulcanizing agent (1-6 parts by weight) is additioned in the fluorinated elastomer (100 parts by weight), before adding the acid acceptor (2-10 parts by weight), with the basic compounds (1-7 parts by weight), the reinforcing and inert fillers, the lubricants, the plasticizers and other optional additives.
  • the fluorinated elastomers obtained from the compositions of the present invention are utilizable as sealing gaskets, in both static and dynamic conditions, in the motorized, mechanical, naval fields, as protective garments for the contact with aggressive chemical agents, as sheaths which protect electrical cables when exposed to an intense thermal radiation, and in other similar appliances.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US06/591,994 1983-03-22 1984-03-21 Accelerators for vulcanizing vinylidene fluoride elastomeric copolymers Expired - Fee Related US4501858A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT20196/83A IT1163158B (it) 1983-03-22 1983-03-22 Acceleranti per la vulcanizzazione di copolimeri elastomerici
IT20196A/83 1983-03-22

Publications (1)

Publication Number Publication Date
US4501858A true US4501858A (en) 1985-02-26

Family

ID=11164628

Family Applications (1)

Application Number Title Priority Date Filing Date
US06/591,994 Expired - Fee Related US4501858A (en) 1983-03-22 1984-03-21 Accelerators for vulcanizing vinylidene fluoride elastomeric copolymers

Country Status (4)

Country Link
US (1) US4501858A (it)
EP (1) EP0120462B1 (it)
DE (1) DE3466005D1 (it)
IT (1) IT1163158B (it)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61195146A (ja) * 1985-02-25 1986-08-29 Asahi Chem Ind Co Ltd フルオロエラストマ−加硫組成物
US4663395A (en) * 1985-07-25 1987-05-05 E. I. Du Pont De Nemours And Company Fluoroelastomer composition containing accelerator
US4673715A (en) * 1985-07-25 1987-06-16 E. I. Du Pont De Nemours And Company Fluoroelastomer composition containing accelerator
US4748208A (en) * 1984-11-22 1988-05-31 Asahi Kasei Kogyo Kabushiki Kaisha Curable elastomer composition
US4894418A (en) * 1985-11-15 1990-01-16 Ausimont S.P.A. Vulcanizable compositions of fluoroelastomers having improved characteristics of processability and of chemical stability
US5371143A (en) * 1989-11-16 1994-12-06 Minnesota Mining And Manufacturing Company Polymer blend composition of fluorinated elastomers, thermoplastic polymers and thermoplastics elastomers
US5532026A (en) * 1991-12-27 1996-07-02 Taiho Kogyo Co., Ltd. Method of manufacturing a metal gasket
US6117508A (en) * 1997-06-27 2000-09-12 Dyneon Llc Composite articles including a fluoropolymer blend
US6346328B1 (en) 1998-07-30 2002-02-12 Dyneon Llc Composite articles including a fluoropolymer
US20140077462A1 (en) * 2012-09-17 2014-03-20 Hyundai Motor Company Integrated fluorine gasket manufactured by injection molding for hydrogen fuel cells
US10358551B2 (en) 2010-07-20 2019-07-23 Solvay Specialty Polymers Italy S.P.A. Fluoroelastomer composition

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6286044A (ja) * 1985-10-11 1987-04-20 Asahi Glass Co Ltd 加硫可能な組成物
US4732958A (en) * 1986-12-30 1988-03-22 Shell Oil Company Epoxy fusion process
US4912171A (en) * 1988-04-01 1990-03-27 Minnesota Mining And Manufacturing Company Fluoroelastomer curing process with phosphonium compound
US5478652A (en) * 1989-06-22 1995-12-26 Minnesota Mining And Manufacturing Company Fluoroelastomer composition with improved bonding properties
US5284611A (en) * 1989-06-22 1994-02-08 Minnesota Mining And Manufacturing Company Fluoroelastomer composition with improved bonding properties
IT1255633B (it) * 1992-05-22 1995-11-09 Ausimont Spa Copolimeri fluoroelastomerici e fluoroplastomerici dotati di elevata resistenza alle basi
US5262490A (en) * 1992-08-24 1993-11-16 Minnesota Mining And Manufacturing Company Fluoroelastomer composition with organo-onium compounds
IT1255853B (it) * 1992-10-12 1995-11-17 Ausimont Spa Composizioni di polimeri elastomerici vulcanizzabili per via ionica
IT1265461B1 (it) * 1993-12-29 1996-11-22 Ausimont Spa Fluoroelastomeri comprendenti unita' monomeriche derivanti da una bis-olefina
IT1273608B (it) * 1995-04-28 1997-07-08 Ausimont Spa Fluoroelastomeri sostanzialmente privi di terminali polari e relativo processo di preparazione
IT1286042B1 (it) * 1996-10-25 1998-07-07 Ausimont Spa O-rings da fluoroelastomeri vulcanizzabili per via ionica
US6087406A (en) * 1997-03-12 2000-07-11 Dyneon Llc Recycle of vulcanized fluorinated elastomers
IT1292361B1 (it) 1997-05-20 1999-01-29 Ausimont Spa Composizioni fluoroelastomeriche volcanizzabili
KR20010079757A (ko) 1998-09-08 2001-08-22 조나쏜 지. 란데 다층 복합재
US7534845B2 (en) 2000-04-21 2009-05-19 Solvay Solexis S.P.A. Fluorovinyl ethers and polymers obtainable therefrom
IT1318488B1 (it) 2000-04-21 2003-08-25 Ausimont Spa Fluorovinileteri e polimeri da essi ottenibili.
IT1318487B1 (it) 2000-04-21 2003-08-25 Ausimont Spa Fluoroelastomeri.
ITMI20011059A1 (it) 2001-05-22 2002-11-22 Ausimont Spa Composizioni fluoroelastomeriche
ITMI20011062A1 (it) 2001-05-22 2002-11-22 Ausimont Spa Composizioni fluoroelastomeriche
ITMI20012164A1 (it) 2001-10-18 2003-04-18 Ausimont Spa Fluoroelastomeri
ITMI20020598A1 (it) 2002-03-22 2003-09-22 Ausimont Spa Fluoroelastomeri vulcanizzabili
ITMI20040830A1 (it) 2004-04-27 2004-07-27 Solvay Solexis Spa Fluoroelastomeri vulcanizzabili
ITMI20041253A1 (it) 2004-06-22 2004-09-22 Solvay Solexis Spa Gel di fluoroelastomeri
ITMI20041573A1 (it) 2004-07-30 2006-01-31 Solvay Solexis Spa Fluoroelastomeri
WO2008080897A1 (en) 2007-01-03 2008-07-10 Solvay Solexis, Inc. Fluoroelastomer composition
US8242210B2 (en) 2007-08-29 2012-08-14 Solvay Solexis S.P.A. (Per)fluoroelastomeric compositions
EP2065441A1 (en) 2007-11-30 2009-06-03 Solvay Solexis S.p.A. Fluoroelastomer composition
EP2373735B1 (en) 2008-12-05 2015-04-01 Solvay Specialty Polymers Italy S.p.A. Vulcanized (per)fluoroelastomer sealing articles
EP2194094A1 (en) 2008-12-08 2010-06-09 Solvay Solexis S.p.A. (Per)fluoroelastomer composition
CN102770468B (zh) 2009-12-18 2016-08-10 索尔维特殊聚合物意大利有限公司 用于生产氟弹性体的方法
WO2012007374A1 (en) 2010-07-14 2012-01-19 Solvay Solexis S.P.A. Fluoroelastomer composition
EP2627683B1 (en) 2010-10-15 2014-08-13 Solvay Specialty Polymers Italy S.p.A. Fluoroelastomers
CN103370346B (zh) 2010-12-20 2016-12-14 索尔维特殊聚合物意大利有限公司 低粘度氟弹性体
EP2705061B1 (en) 2011-05-03 2017-02-01 Solvay Specialty Polymers Italy S.p.A. Method for manufacturing fluoroelastomers
EP2718338B1 (en) 2011-06-09 2017-10-25 Solvay Specialty Polymers Italy S.p.A. Hyperbranched fluoroelastomer additive
JP6530191B2 (ja) 2011-08-17 2019-06-12 ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. ミリング方法
WO2014206955A1 (en) 2013-06-28 2014-12-31 Solvay Specialty Polymers Italy S.P.A. Fluoroelastomers
EP3350237B1 (en) 2015-09-18 2020-07-08 Solvay Specialty Polymers Italy S.p.A. Fluoroelastomer composition
WO2017102818A1 (en) 2015-12-14 2017-06-22 Solvay Specialty Polymers Italy S.P.A. Fluoroelastomer compositions
ES2951768T3 (es) 2017-06-30 2023-10-24 Solvay Specialty Polymers It Método para fabricar polímeros parcialmente fluorados
JP7321168B2 (ja) 2018-02-12 2023-08-04 ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. フルオロエラストマー硬化性組成物
EP3873985A1 (en) 2018-10-31 2021-09-08 Solvay Specialty Polymers Italy S.p.A. Curable composition of elastomers
JP7555952B2 (ja) 2019-03-20 2024-09-25 ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. フルオロエラストマー組成物
JP2022540646A (ja) 2019-07-17 2022-09-16 ソルベイ スペシャルティ ポリマーズ イタリー エス.ピー.エー. ポリアミドとフルオロエラストマーとを含む複合材料
WO2021224164A1 (en) 2020-05-07 2021-11-11 Solvay Specialty Polymers Italy S.P.A. Polyamide/fluoroelastomer blends and corresponding articles and formation methods
US20240186522A1 (en) 2021-03-22 2024-06-06 Solvay Specialty Polymers Italy S.P.A. Composition for electrodes

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3752787A (en) * 1972-01-28 1973-08-14 Du Pont Fluoroelastomer composition containing a triarylphosphorane vulcanization accelerator
US4243770A (en) * 1977-04-08 1981-01-06 Daikin Kogyo Co., Ltd. Cross linkable fluorine-containing polymer and its production
US4259463A (en) * 1977-12-14 1981-03-31 Montedison S.P.A. Vulcanizable compositions based on copolymers of vinylidene fluoride and containing vulcanization accelerators which are aminophosphinic compounds

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3752787A (en) * 1972-01-28 1973-08-14 Du Pont Fluoroelastomer composition containing a triarylphosphorane vulcanization accelerator
US4243770A (en) * 1977-04-08 1981-01-06 Daikin Kogyo Co., Ltd. Cross linkable fluorine-containing polymer and its production
US4259463A (en) * 1977-12-14 1981-03-31 Montedison S.P.A. Vulcanizable compositions based on copolymers of vinylidene fluoride and containing vulcanization accelerators which are aminophosphinic compounds

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
"Reactions of Benzylic Compounds, (etc.)" Maartmen-Mae et al., Acta Chem. Scan., B 36 (1982), 211-223.
"The Solution Properties of Bis(Triphenylphosphine) Iminium Salts," Palmesen et al., Acta Chem. Scan. A35, 1981, 803-809.
Reactions of Benzylic Compounds, (etc.) Maartmen Mae et al., Acta Chem. Scan., B 36 (1982), 211 223. *
The Solution Properties of Bis(Triphenylphosphine) Iminium Salts, Palmesen et al., Acta Chem. Scan. A35, 1981, 803 809. *

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4748208A (en) * 1984-11-22 1988-05-31 Asahi Kasei Kogyo Kabushiki Kaisha Curable elastomer composition
JPS61195146A (ja) * 1985-02-25 1986-08-29 Asahi Chem Ind Co Ltd フルオロエラストマ−加硫組成物
US4663395A (en) * 1985-07-25 1987-05-05 E. I. Du Pont De Nemours And Company Fluoroelastomer composition containing accelerator
US4673715A (en) * 1985-07-25 1987-06-16 E. I. Du Pont De Nemours And Company Fluoroelastomer composition containing accelerator
US4894418A (en) * 1985-11-15 1990-01-16 Ausimont S.P.A. Vulcanizable compositions of fluoroelastomers having improved characteristics of processability and of chemical stability
US5371143A (en) * 1989-11-16 1994-12-06 Minnesota Mining And Manufacturing Company Polymer blend composition of fluorinated elastomers, thermoplastic polymers and thermoplastics elastomers
US5532026A (en) * 1991-12-27 1996-07-02 Taiho Kogyo Co., Ltd. Method of manufacturing a metal gasket
US6117508A (en) * 1997-06-27 2000-09-12 Dyneon Llc Composite articles including a fluoropolymer blend
USRE40516E1 (en) 1997-06-27 2008-09-23 3M Innovative Properties Company Composite articles including a fluoropolymer blend
US6346328B1 (en) 1998-07-30 2002-02-12 Dyneon Llc Composite articles including a fluoropolymer
US10358551B2 (en) 2010-07-20 2019-07-23 Solvay Specialty Polymers Italy S.P.A. Fluoroelastomer composition
US20140077462A1 (en) * 2012-09-17 2014-03-20 Hyundai Motor Company Integrated fluorine gasket manufactured by injection molding for hydrogen fuel cells
US9640807B2 (en) * 2012-09-17 2017-05-02 Hyundai Motor Company Integrated fluorine gasket manufactured by injection molding for hydrogen fuel cells

Also Published As

Publication number Publication date
IT1163158B (it) 1987-04-08
IT8320196A0 (it) 1983-03-22
EP0120462A1 (en) 1984-10-03
EP0120462B1 (en) 1987-09-09
DE3466005D1 (en) 1987-10-15

Similar Documents

Publication Publication Date Title
US4501858A (en) Accelerators for vulcanizing vinylidene fluoride elastomeric copolymers
US4259463A (en) Vulcanizable compositions based on copolymers of vinylidene fluoride and containing vulcanization accelerators which are aminophosphinic compounds
US3686143A (en) Guanidine and amidine accelerators for vulcanization of fluoroelastomers
CA1328533C (en) Fluoroelastomer composition
JP2517248B2 (ja) 加工性および化学安定性の改良特性を有するフルオロエラストマ−の加硫性組成物
US3945966A (en) Vulcanization of fluoroalkoxyphosphazene polymers
JP2527946B2 (ja) フルオロエラストマ−の加硫性エラストマ−組成物
JPS6252772B2 (it)
US3692732A (en) Curable polyorganosiloxane elastomers and process for curing same
CN1159370C (zh) 用铜盐和芳族卤素化合物稳定的聚酰胺组合物
CA1049687A (en) Vulcanizable compositions based on elastomeric copolymers of vinylidene fluoride, vulcanization process thereof and vulcanized compositions thus obtained
US3806488A (en) Stabilized flame resistant polyamides
CA1040335A (en) Curable compositions based on elastomeric vinylidene fluoride copolymers, process for curing the compositions, and the cured compositions
JPS6183255A (ja) 室温硬化性オルガノポリシロキサン組成物およびその製造方法
US3872054A (en) Flame retardant room temperature vulcanizing organopolysiloxane composition
JPS6054976B2 (ja) ハロゲン含有ポリマ−加硫用組成物
US6534576B2 (en) Flame retardant organic resin composition
CA1155250A (en) Oxygen-curable mercaptoorganosiloxane compositions catalyzed by metal carbonyl compounds and method of forming higher molecular weight products therefrom
US3468838A (en) Silicone rubber materials
JPS603427B2 (ja) レドツクス化合物および鉄カルボニル化合物の両者を含む酸素硬化性メルカプトオルガノシロキサン組成物およびそれから高分子量生成物を製造する方法
US20070272903A1 (en) Arylalkylsilyls Used as a Flame Retardant Additives
EP0344771A1 (en) Inhibition of poly(arylene sulfide) resin induced metal corrosion
CA1115886A (en) Stabilization of polyphosphazene vulcanizates
CN102532858A (zh) 磷腈化合物阻燃聚碳酸酯组合物
JPH0218332B2 (it)

Legal Events

Date Code Title Description
AS Assignment

Owner name: MONTEDISON S.P.A. MILANO ITALY 31, FORO BUONAPARTE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MOGGI, GIOVANNI;REEL/FRAME:004242/0523

Effective date: 19840308

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
FP Lapsed due to failure to pay maintenance fee

Effective date: 19930228

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362